*Optimal dilutions/concentrations should be determined by the researcher.
|~0.5 μg /ml
Not tested in other applications.
We do not recommend use of this product for Mouse.
Filter-sterilized PBS, 50% glycerol
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
1 mg/ml (Please refer to the vial label for the specific concentration.)
Recombinant human PrP lacking GPI anchor expressed and purified from rabbit kidney cell line RK13
For laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.
prion protein , ASCR , AltPrP , CD230 , CJD , GSS , KURU , PRIP , PRNP , PrP , PrP2730 , PrP3335C , PrPc , p2730 , Prion protein PrP
Mitochondrion outer membrane,Cell membrane,Golgi apparatus,Cytoplasm,Nucleus
The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that tends to aggregate into rod-like structures. The encoded protein contains a highly unstable region of five tandem octapeptide repeats. This gene is found on chromosome 20, approximately 20 kbp upstream of a gene which encodes a biochemically and structurally similar protein to the one encoded by this gene. Mutations in the repeat region as well as elsewhere in this gene have been associated with Creutzfeldt-Jakob disease, fatal familial insomnia, Gerstmann-Straussler disease, Huntington disease-like 1, and kuru. An overlapping open reading frame has been found for this gene that encodes a smaller, structurally unrelated protein, AltPrp. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]